PRSice2 Development of risk score

Step 0: Prepare covariates and input files

IDs <- fread("~/genotype_qc/TERRE_QC/all_imputed_r2_30_rsid_hard_call.fam")[, .(FID = V1, IID = V2)]
prsice_cov <- fread("prsice_cov_and_status_mvalues.txt")
prsice_cov <- prsice_cov[match(IDs$IID,prsice_cov$IID)]
all(IDs$IID ==prsice_cov$IID)

[1] NA

covariate <- cbind(IDs, prsice_cov[,-c(16,17,18)])

PD <- cbind(IDs,prsice_cov[,16])

head(covariate)

head(PD)

fwrite(na.omit(PD), "TERRE.pheno", sep = "\t")
fwrite(na.omit(covariate), "TERRE.covariate", sep = "\t")

covariate

Step 1: Run PRSice-2 on Nalls et al 2019 Sumstats

Rscript /home1/NEURO/casazza/PRSice.R \
    --prsice /home1/NEURO/casazza/PRSice_linux\
    --base /home1/NEURO/casazza/nalls_PD.QC.gz\
    --base-info INFO:0.8 \
    --base-maf MAF:0.01 \
    --cov TERRE.covariate \
    --binary-target T\
    --beta  \
    --ld /home1/NEURO/casazza/1000G_plink/EUR_phase3  \
    --out TERRE_PRSice \
    -q 5\
    --all-score\
    --pheno TERRE.pheno \
    --snp SNP \
    --stat b \
    --pvalue p\
    --target /home1/NEURO/casazza/genotype_qc/TERRE_QC/all_imputed_r2_30_rsid_hard_call \
    --thread 32

Step 2: Evaluate output

include_graphics("prsice_images/TERRE_PRSice_BARPLOT_2022-06-30.png")

include_graphics("prsice_images/TERRE_PRSice_HIGH-RES_PLOT_2022-06-30.png")

include_graphics("prsice_images/TERRE_PRSice_QUANTILES_PLOT_2022-06-30.png")

include_graphics("prsice_images/TERRE_PRSice_nalls_male_BARPLOT_2022-10-04.png")

include_graphics("prsice_images/TERRE_PRSice_nalls_male_HIGH-RES_PLOT_2022-10-04.png")

include_graphics("prsice_images/TERRE_PRSice_nalls_male_QUANTILES_PLOT_2022-10-04.png")

include_graphics("prsice_images/TERRE_PRSice_nalls_female_BARPLOT_2022-10-04.png")

include_graphics("prsice_images/TERRE_PRSice_nalls_female_HIGH-RES_PLOT_2022-10-04.png")

include_graphics("prsice_images/TERRE_PRSice_nalls_female_QUANTILES_PLOT_2022-10-04.png")

Plotting PRSice Data on my own

library(ggnewscale)
prsice_male_meta <- fread("prsice_nalls_male_data/TERRE_PRSice_nalls_male.prsice")
ggplot(prsice_male_meta[Threshold <= 0.5], aes(Threshold, Num_SNP, color = -log10(P))) +
  geom_point() +
  scale_y_continuous(breaks = c(seq(0, 1e5, 2.5e4), seq(2e5, 6e5, 1e5))) +
  theme_minimal()

prsice_female_meta <- fread("prsice_nalls_female_data/TERRE_PRSice_nalls_female.prsice")
ggplot(prsice_female_meta[Threshold <= 0.5], aes(Threshold, Num_SNP, color = -log10(P))) +
  geom_point() +
  scale_y_continuous(breaks = c(seq(0, 1e5, 2.5e4), seq(2e5, 6e5, 1e5))) +
  theme_minimal()

prsice_meta <- fread("prsice_data/TERRE_PRSice.prsice")
ggplot(mapping = aes(Threshold, R2, color = -log10(P))) +
  geom_point(data = prsice_female_meta, size = 1) +
  scale_color_gradient(low = "lightpink4", high = "lightpink") +
  labs(color = bquote("Female log"["10"] ~ "(P)")) +
  new_scale_color() +
  geom_point(data = prsice_male_meta, size = 1, aes(color = -log10(P))) +
  scale_color_gradient(low = "lightblue4", high = "lightblue") +
  labs(y = bquote("R"^2), x = "GWAS P-Value Threshold", color = bquote("Male -log"["10"] ~ "(P)")) +
  theme_minimal() +
  theme(legend.position = "top")

ggplot(mapping = aes(Threshold, R2, color = -log10(P))) +
  geom_point(data = prsice_female_meta, size = 1) +
  scale_color_gradient(low = "lightpink4", high = "lightpink",guide = guide_colorbar(order=3)) +
  labs(color = bquote("Female -log"["10"] ~ "(P)")) +
  new_scale_color() +
  geom_point(data = prsice_male_meta, size = 1, aes(color = -log10(P))) +
  scale_color_gradient(low = "lightblue4", high = "lightblue",guide = guide_colorbar(order=2)) +
  labs(color = bquote("Male -log"["10"] ~ "(P)")) +
  new_scale_color() +
  geom_point(data = prsice_meta, size = 1, aes(color = -log10(P))) +
  scale_color_gradient(low = "gray40", high = "gray80",guide = guide_colorbar(order=1)) +
  labs(y = bquote("R"^2), x = "GWAS P-Value Threshold", color = bquote("Cross-sex -log"["10"] ~ "(P)")) +
  theme_minimal() +
  theme(legend.position = "top",legend.title = element_text(size=7))

Step 3 run linear model at different thresholds for SNP inclusion

This is updated to recently processed DNAm Data 20 outliers in DNAm removed:

load("/home1/NEURO/SHARE_DECIPHER/processed_DNAm_data/2022/TERRE_processed_2022/1-TERRE_RG_filtered.RData") #PD_RG_filtered
# Assign genotyping ID to data
original_covars <- fread("/home1/NEURO/SHARE_DECIPHER/terre_meta_master.csv")[, .(patient, IID = gsub("_PAE.*", "", IID))]
betas_combat <- minfi::getBeta(PD_RG_filtered)
colnames(betas_combat) <- original_covars$IID[match(colnames(betas_combat), original_covars$patient)]
betas_combat <- betas_combat[, colnames(betas_combat) %in% covariate$IID]

Let’s check how the data looks for the first 5 subjects:

ggplot(betas_combat[, 1:5] %>% as.data.table(keep.rownames = T) %>% melt(id.vars = "rn", value.name = "betas", variable.name = "subject"), aes(betas, color = subject))+
  geom_density()

Match DNA, PRS, and metadata @TODO fix this after update of PRS etc.

prsice_best <- fread("prsice_data/TERRE_PRSice.best")[match(colnames(betas_combat), IID,nomatch=0),.(best=PRS)]
prsice_all <- cbind(
  fread("prsice_data/TERRE_PRSice.all_score")[match(colnames(betas_combat), IID,nomatch=0), .(FID, IID, `Pt_5e-08`, `Pt_5.005e-05`, `Pt_0.00010005`, `Pt_0.00100005`, `Pt_0.0101501`, `Pt_0.1`, `Pt_0.2`, `Pt_0.3`, `Pt_0.4`, `Pt_0.5`, `Pt_1`)],
  prsice_best
)
covariate <- covariate[match(colnames(betas_combat), IID)]
all(covariate$IID == colnames(betas_combat))

[1] TRUE

all(covariate$IID == prsice_all$IID)

[1] TRUE

covariate_male <- covariate[sex == 1] %>% select(-sex)
betas_male <- betas_combat[, covariate_male$IID]
prsice_male_best <- fread("prsice_nalls_male_data/TERRE_PRSice_nalls_male.best")[match(colnames(betas_male), IID,nomatch=0),.(best=PRS)]
prsice_male_all <- cbind(
  fread("prsice_nalls_male_data/TERRE_PRSice_nalls_male.all_score")[match(colnames(betas_male), IID,nomatch=0), .(FID, IID, `Pt_5e-08`, `Pt_5.005e-05`, `Pt_0.00010005`, `Pt_0.00100005`, `Pt_0.0101501`, `Pt_0.1`, `Pt_0.2`, `Pt_0.3`, `Pt_0.4`, `Pt_0.5`, `Pt_1`)],
  prsice_male_best
)
covariate_male <- covariate_male[match(colnames(betas_male), IID,nomatch=0)]
all(covariate_male$IID == colnames(betas_male))

[1] TRUE

all(covariate_male$IID == prsice_male_all$IID)

[1] TRUE

prsice_female_best <- fread("prsice_nalls_female_data/TERRE_PRSice_nalls_female.best")
covariate_female <- covariate[sex == 0] %>% select(-sex) %>% filter(IID %in% prsice_female_best$IID)
betas_female <- betas_combat[, covariate_female$IID]
prsice_female_best <- prsice_female_best[match(colnames(betas_female), IID,nomatch=0),.(best=PRS)]
prsice_female_all <- cbind(
  fread("prsice_nalls_female_data/TERRE_PRSice_nalls_female.all_score")[match(colnames(betas_female), IID,nomatch=0), .(FID, IID, `Pt_5e-08`, `Pt_5.005e-05`, `Pt_0.00010005`, `Pt_0.00100005`, `Pt_0.0101501`, `Pt_0.1`, `Pt_0.2`, `Pt_0.3`, `Pt_0.4`, `Pt_0.5`, `Pt_1`)],
  prsice_female_best
)
covariate_female <- covariate_female[match(colnames(betas_female), IID,nomatch=0)]
all(covariate_female$IID == colnames(betas_female))

[1] TRUE

all(covariate_female$IID == prsice_female_all$IID)

[1] TRUE

Run limma

mvalues <- lumi::beta2m(betas_combat)
prs_mat <- prsice_all[, -c(1, 2)]
cov_mat <- covariate[, -c(1, 2)]

mvalues_male <- lumi::beta2m(betas_male)
prs_mat_male <- prsice_male_all[, -c(1, 2)]
cov_mat_male <- covariate_male[, -c(1, 2)]

mvalues_female <- lumi::beta2m(betas_female)
prs_mat_female <- prsice_female_all[, -c(1, 2)]
cov_mat_female <- covariate_female[, -c(1, 2)]

registerDoParallel(ncol(prs_mat) / 4)
hits <- foreach(prs_thresh = colnames(prs_mat)) %dopar% {
  design_prs <- model.matrix(~., data = cbind(prs_mat[, ..prs_thresh], cov_mat))
  prs_fit <- lmFit(mvalues, design_prs)
  prs_fit <- eBayes(prs_fit)
  topTable(prs_fit, coef = 2, adjust.method = "bonf", p.value = 0.05, number = Inf, genelist = rownames(mvalues))
}

Plotting EWAS vs Threshold Experiment by Sex

to_plot <- rbind(
  hits_by_thresh_bonf[, .(hits = .N, Sex = "Cross-sex"), by = threshold] %>%
    mutate(threshold = recode_factor(threshold, `Pt_0.0219001` = "0.0219", `Pt_5e-08` = "5e-8", `Pt_5.005e-05` = "5e-5", `Pt_0.00010005` = "1e-4", `Pt_0.00100005` = "1e-3", `Pt_0.0101501` = "1e-2", `Pt_0.1` = "0.1", `Pt_0.2` = "0.2", `Pt_0.3` = "0.3", `Pt_0.4` = "0.4", `Pt_0.5` = "0.5", `Pt_1` = "1.0")),
  hits_by_thresh_bonf_male[, .(hits = .N, Sex = "Male"), by = threshold] %>%
    mutate(threshold = recode_factor(threshold, `Pt_0.0219001` = "0.0219", `Pt_5e-08` = "5e-8", `Pt_5.005e-05` = "5e-5", `Pt_0.00010005` = "1e-4", `Pt_0.00100005` = "1e-3", `Pt_0.0101501` = "1e-2", `Pt_0.1` = "0.1", `Pt_0.2` = "0.2", `Pt_0.3` = "0.3", `Pt_0.4` = "0.4", `Pt_0.5` = "0.5", `Pt_1` = "1.0")),
  hits_by_thresh_bonf_female[, .(hits = .N, Sex = "Female"), by = threshold] %>%
    mutate(threshold = recode_factor(threshold, `Pt_0.0219001` = "0.0219", `Pt_5e-08` = "5e-8", `Pt_5.005e-05` = "5e-5", `Pt_0.00010005` = "1e-4", `Pt_0.00100005` = "1e-3", `Pt_0.0101501` = "1e-2", `Pt_0.1` = "0.1", `Pt_0.2` = "0.2", `Pt_0.3` = "0.3", `Pt_0.4` = "0.4", `Pt_0.5` = "0.5", `Pt_1` = "1.0"))
) %>% mutate(Sex = factor(Sex, levels = c("Cross-sex", "Male", "Female")))
plot_pos <- position_dodge(width = 1)
ggplot(to_plot, aes(threshold, hits, fill = Sex, label = hits)) +
  geom_text(position = plot_pos, vjust = -0.25) +
  geom_col(position = plot_pos) +
  labs(x = "GWAS P Value Threshold", y = "EWAS Hits") +
  scale_fill_manual(values = c("grey80", "lightblue", "lightpink")) +
  theme_minimal()

hits_by_thresh_bonf[, .(hits = .N, Sex = "Cross-sex"), by = threshold]

hits_by_thresh_bonf_male[, .(hits = .N), by = threshold]

hits_by_thresh_bonf_female[, .(hits = .N), by = threshold]

display_venn <- function(x, ...) {
  library(VennDiagram)
  grid.newpage()
  venn_object <- venn.diagram(x, filename = NULL, ...)
  grid.draw(venn_object)
}

display_venn(list(`Cross-sex` = hits_by_thresh_bonf[threshold == "Pt_5e-08"]$ID, Male = hits_by_thresh_bonf_male[threshold == "Pt_5e-08"]$ID, Female = hits_by_thresh_bonf_female[threshold == "Pt_5e-08"]$ID), fill = c("gray80", "lightblue", "lightpink"))

Loading required package: grid
Loading required package: futile.logger

male_ids <- hits_by_thresh_bonf_male[threshold == "Pt_5e-08"]$ID
cross_ids <- hits_by_thresh_bonf[threshold == "Pt_5e-08"]$ID
male_ids[!male_ids %in% cross_ids]

character(0)

get_full_fit <- function(prs_mat,cov_mat,mvalues){
  top_design_prs <- model.matrix(~., data = cbind(prs_mat[, `Pt_5e-08`], cov_mat))
  top_prs_fit <- lmFit(mvalues, top_design_prs)
  top_prs_fit <- eBayes(top_prs_fit)
  top_prs_hits <- topTable(top_prs_fit, coef = 2, adjust.method = "bonf", number = Inf, genelist = rownames(mvalues))
}
top_prs_hits <- get_full_fit(prs_mat,cov_mat,mvalues)
top_male_prs_hits <- get_full_fit(prs_mat_male, cov_mat_male, mvalues_male)
top_female_prs_hits <- get_full_fit(prs_mat_female, cov_mat_female, mvalues_female)
save(list=c("top_prs_hits","top_male_prs_hits","top_female_prs_hits"),file="prs_nalls_cross_w_sex_stratified.RData")

load("prs_nalls_cross_w_sex_stratified.RData")

manifest <- IlluminaHumanMethylationEPICanno.ilm10b4.hg19::Other %>%
  as.data.frame() %>%
  rownames_to_column(var = "name")
prs_annot <- data.table(top_prs_hits)[manifest, gene := gsub(";.*", "", UCSC_RefGene_Name), on = c(ID = "name")]
prs_annot_male <- data.table(top_male_prs_hits)[manifest, gene := gsub(";.*", "", UCSC_RefGene_Name), on = c(ID = "name")]
prs_annot_female<- data.table(top_female_prs_hits)[manifest, gene := gsub(";.*", "", UCSC_RefGene_Name), on = c(ID = "name")]
plot_prs_hits <- function(prs_annot,label_color){
  ggplot(prs_annot, aes(logFC, -log10(P.Value))) +
    geom_point() +
    geom_point(
      data = subset(prs_annot, adj.P.Val < 0.05 & abs(logFC) > 0.03),
      color = label_color,
      mapping = aes(logFC, -log10(P.Value))
    ) +
    geom_hline(
      linetype = "dashed",
      yintercept = min(-log10(prs_annot$P.Value[prs_annot$adj.P.Val < 0.05]))
    ) +
    geom_vline(linetype = "dashed", xintercept = 0.03) +
    geom_vline(linetype = "dashed", xintercept = -0.03) +
    geom_text_repel(
      data = prs_annot %>% filter(abs(logFC) > 0.03 & adj.P.Val < 0.05),
      color = "dodgerblue",
      mapping = aes(logFC, -log10(P.Value), label = ifelse(gene != "", gene, ID)),
      size = 3,
      max.overlaps = 20
    ) +
    labs(y = bquote("log"[10] ~ "(P)"), x = quote(Delta ~ "M" ~ Methylation)) +
    theme_minimal()
}

plot_prs_hits(prs_annot,"gray40")

plot_prs_hits(prs_annot_male,"lightblue")

plot_prs_hits(prs_annot_female,"pink")

go enrichment?

library(gprofiler2)
cross_sex <- unique(gsub(";.*","",manifest[manifest$name %in% hits_by_thresh_bonf[threshold == "Pt_5e-08"]$ID,]$UCSC_RefGene_Name))
background <- unique(gsub(";.*","",manifest$UCSC_RefGene_Name))
gost_res <- gost(query=cross_sex,custom_bg = background)
gostplot(gost_res)

gmirror(
  prs_annot_male[,.(SNP=ID,CHR=gsub("chr","",cpg_pos[match(ID,cpg_pos$name),]$chr),POS=cpg_pos[match(ID,cpg_pos$name),]$pos,pvalue=P.Value)],
  prs_annot_female[,.(SNP=ID,CHR=gsub("chr","",cpg_pos[match(ID,cpg_pos$name),]$chr),POS=cpg_pos[match(ID,cpg_pos$name),]$pos,pvalue=P.Value)],
  annotate_snp = c(male_annot_cpg,female_annot_cpg),
  tline =  max(prs_annot_male[adj.P.Val<0.25]$P.Value),
  bline =  max(prs_annot_female[adj.P.Val<0.25]$P.Value),
  highlight_p = c(max(prs_annot_male[adj.P.Val<0.25]$P.Value),max(prs_annot_female[adj.P.Val<0.25]$P.Value)),
  toptitle="Male",
  bottomtitle ="Female",
  highlighter="green",
  background="white"
)

[1] "Saving plot to gmirror.png"
TableGrob (2 x 1) "arrange": 2 grobs

Manhattan plot vs GWAS manhattan plot

library(qqman)

copy_annot <- prs_annot[cpg_pos, on = c(ID = "name")] %>%
  mutate(chr = as.numeric(recode(gsub("chr", "", chr),X="23",Y="24")))
to_plot <- copy_annot[, .(SNP = gene, CHR = chr, BP = pos, P = P.Value, FDR = adj.P.Val)][!is.na(P)]
manhattan(to_plot,
  annotatePval = max(to_plot[FDR < 0.05]$P),
  annotateTop = TRUE,
  genomewideline = min(-log10(to_plot[FDR < 0.05]$P)),
  suggestiveline = FALSE
)
manhattan(to_plot[CHR == 17],
  annotatePval = max(to_plot[FDR < 0.05]$P),
  annotateTop = FALSE,
  genomewideline = min(-log10(to_plot[FDR < 0.05]$P)),
  suggestiveline = FALSE
)
qq(to_plot$P)

DMRs

library(DMRcate)

Loading required package: minfi
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Attaching package: ‘BiocGenerics’

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    pmax.int, pmin, pmin.int, Position, rank, rbind, Reduce, rownames, sapply, setdiff, sort, table, tapply, union,
    unique, unsplit, which, which.max, which.min

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replacing previous import 'minfi::getMeth' by 'bsseq::getMeth' when loading 'DMRcate'

S4_to_dataframe <- function(s4obj) {
  nms <- slotNames(s4obj)
  lst <- lapply(nms, function(nm) slot(s4obj, nm))
  as.data.frame(setNames(lst, nms))
}
run_dmrcate <- function(prs_mat,cov_mat,mvalues){
  design_prs <- model.matrix(~., data = cbind(prs_mat[, `Pt_5e-08`], cov_mat))
  prs_annotated <- cpg.annotate(datatype = "array", object = mvalues, analysis.type = "differential", design = design_prs, coef = 2, what = "M", arraytype = "EPIC", fdr = 0.05)
  prs_dmr_res <- dmrcate(prs_annotated, lambda = 1000, C = 2)
  return(S4_to_dataframe(prs_dmr_res))
}
dmr_cross <- run_dmrcate(prs_mat, cov_mat, mvalues)

Loading required package: IlluminaHumanMethylationEPICanno.ilm10b4.hg19
Your contrast returned 85 individually significant probes; a small but real effect. Consider manually setting the value of pcutoff to return more DMRs, but be warned that doing this increases the risk of Type I errors.
Fitting chr1...
Fitting chr2...
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Fitting chrX...
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Demarcating regions...
Done!

dmr_males <- run_dmrcate(prs_mat_male,cov_mat_male,mvalues_male)

Your contrast returned 59 individually significant probes; a small but real effect. Consider manually setting the value of pcutoff to return more DMRs, but be warned that doing this increases the risk of Type I errors.
Fitting chr1...
Fitting chr2...
Fitting chr3...
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Fitting chr14...
Fitting chr15...
Fitting chr16...
Fitting chr17...
Fitting chr18...
Fitting chr19...
Fitting chr20...
Fitting chr21...
Fitting chr22...
Fitting chrX...
Fitting chrY...
Demarcating regions...
Done!

dmr_female <- run_dmrcate(prs_mat_female,cov_mat_female,mvalues_female)

Your contrast returned 41 individually significant probes; a small but real effect. Consider manually setting the value of pcutoff to return more DMRs, but be warned that doing this increases the risk of Type I errors.
Fitting chr1...
Fitting chr2...
Fitting chr3...
Fitting chr4...
Fitting chr5...
Fitting chr6...
Fitting chr7...
Fitting chr8...
Fitting chr9...
Fitting chr10...
Fitting chr11...
Fitting chr12...
Fitting chr13...
Fitting chr14...
Fitting chr15...
Fitting chr16...
Fitting chr17...
Fitting chr18...
Fitting chr19...
Fitting chr20...
Fitting chr21...
Fitting chr22...
Fitting chrX...
Fitting chrY...
Demarcating regions...
Done!

annotation <- minfi::getAnnotation(IlluminaHumanMethylationEPICanno.ilm10b4.hg19)

Plotting all DMRs

get_dmr_effects <- function(dmr, limma_res,mvalues) {
  dmr_coord <- str_match_all(as.character(dmr), "(chr.*):([0-9]*)-([0-9]*)")[[1]]
  cpgs <- as.data.table(annotation[annotation$chr == dmr_coord[2] & annotation$pos >= as.numeric(dmr_coord[3]) & annotation$pos <= as.numeric(dmr_coord[4]), ])
  res <- limma_res[cpgs,on=c("ID"="Name"),nomatch=0 ]
  dmr_1 <- as.data.frame(res[!is.na(res$logFC), ])
  dmr_methy <- reshape2::melt(lumi::m2beta(mvalues[dmr_1$ID, ]), stringsAsFactors = FALSE)
  to_plot <- merge(dmr_1, dmr_methy, by.x = "ID", by.y = "Var1")
  to_plot$DMR <- dmr
  to_plot
}
get_dmr_res <- function(dmr, limma_res) {
  dmr_coord <- str_match_all(as.character(dmr), "(chr.*):([0-9]*)-([0-9]*)")[[1]]
  cpgs <- annotation[annotation$chr == dmr_coord[2] & annotation$pos >= as.numeric(dmr_coord[3]) & annotation$pos <= as.numeric(dmr_coord[4]), ]
  res <- cbind(cpgs, limma_res[cpgs$Name, ])
  res$DMR <- dmr
  return(res)
}
plot_dmrs <- function(dmr_res,limma_res,prs_mat, mvalues, case_control) {
  to_plot <- rbindlist(lapply(dmr_res$coord, function(dmr) get_dmr_effects(dmr, limma_res,mvalues))) %>%
    mutate(SCORE1_AVG = scale(prs_mat[match(Var2,IDs$IID),`Pt_5e-08`]),PD = PD[match(Var2,IID)]$PD) %>%
    filter(!is.na(SCORE1_AVG))
  for(cur_dmr in unique(to_plot$DMR)){
    cur_plot <- to_plot[DMR == cur_dmr]
    p1 <- ggplot(cur_plot , aes(pos, value, color = SCORE1_AVG)) +
      geom_point() +
      scale_color_gradient(low = rev(case_control)[1], high = rev(case_control)[2]) +
      theme_minimal() +
      labs(title = unique(cur_plot$DMR),x="POS",y=bquote("Methylation"~beta),color = "Normalized PD PRS")+
      theme(axis.text.x = element_text(angle = 90))
    p2 <- ggplot(cur_plot %>% mutate(PD = ifelse(PD == 1, "CASE", "CONTROL")), aes(factor(pos), value, color = PD)) +
      geom_boxplot(position = position_dodge(0.75)) +
      scale_color_manual(values = case_control) +
      theme_minimal() +
      stat_summary(aes(group = PD), fun = mean, geom = "line") +
      labs(title = unique(cur_plot$DMR),x="POS",y=bquote("Methylation"~beta),color = "PD status") +
      theme(axis.text.x = element_text(angle = 90))
    print(p1)
    print(p2)
  }
}

plot_dmrs(dmr_cross, prs_annot, prs_mat,mvalues, rev(c("gray80", "gray40")))

plot_dmrs(dmr_males,prs_annot_male,prs_mat_male, mvalues_male,rev(c("light blue", "lightblue4")))

plot_dmrs(dmr_female, prs_annot_female, prs_mat_female, mvalues_female,rev(c("lightpink", "lightpink4")))

dmr_cross

dmr_males

dmr_female

save(list=c("dmr_cross","dmr_males","dmr_female"),file="prs_dmr_nalls.RData")